Divalproex Sodium 65862-0403-22
- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 24, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA090554
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Divalproex Sodium | 500 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]
Selected Package
65862-0403-22Selected2000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-22)
Other packages for this product(3)
100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-01)
500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-05)
10 BLISTER PACK in 1 CARTON (65862-403-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK